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Day 1


Day One: Monday, January 30

10:00 am Summit Registration

OPENING PLENARY KEYNOTE SESSION
Macro Challenges and Strategic Solutions in Drug Discovery & Development

11:00 am Summit Welcome and Opening Address
Perspectives on Attrition Across the R&D Continuum

• Review of survey results about the principal causes of attrition 
• Potential approaches for addressing attrition causes through the different stages of R&D
Chris Clement, Director, Head of Project Office, Millennium Pharmaceuticals
Jan Malek, PA Consulting

 

11:30 am The Use of Portfolio Management, Therapeutic Area Strategy and Biomarkers to Reduce Attrition in Drug Development
• Define the problem — what are the factors impacting productivity with special
  reference on attrition in drug development and a root cause analysis of     attrition. 
• Propose solutions - review the levers for increasing R&D productivity in
  general and attrition in particular. 
• Focus on three levers for solving R&D productivity and especially attrition: 
  
w Therapeutic Areas 
  
w Biomarkers 
• Portfolio Management 
• Model and quantify the possible impact of using these levers to increase R&D productivity/decrease attrition
Ismail Kola, Ph.D., Senior Vice President, Site Head for Basic Research, Rahway, Merck Research Laboratories

 

12:15 pm Balancing the R&D Model to Address Challenges within our Industry Today
Catherine Strader, Ph.D., Executive Vice President, Discovery Research, Schering Plough Research Institute 

1:00 pm Opening Luncheon (Sponsorship Available)

 

2:15 pm Improving R&D by Addressing Bottlenecks for NCEs and NBEs in the Drug Discovery Process
• Risk-balancing the pipeline 
• Exploiting the technology cycles 
• Diversified lead generation 
• Innovation by pathway repositioning
Mikael Dolsten, M.D., Ph.D., Head of Corporate Division Pharma Research, Boehringer
Ingelheim Pharmaceuticals, Inc.

EXECUTIVE ROUNDTABLE DISCUSSIONS

3:00 pm Executive Roundtables
Concurrent round tables to discuss some of the more broad yet, poignant questions facing the industry. Each roundtable will be limited to twelve (12) participants and a facilitator. Additional roundtables and facilitators will be added to accomodate demand for specific topics that attract more than 12 participants.

Roundtable 1: Strategic and Decision-Making Improvements for Phase 2 Survival
Facilitator: Shama Kajiji, Ph.D., MBA, Director, Worldwide Project Management, Head, Attrition Analysis Office, PGRD, Pfizer

Roundtable 2: What Should the Industry Look Like in 20 Years and How Do We Get There?
Facilitator: Rainer Fuchs, Ph.D., Co-Head of Discovery Research, Biogen Idec Inc.

Roundtable 3: How Can Tomograms of Proteins Assist in Selecting the Right Projects for Clinical Development?
Facilitator: Anders Εberg, CSO, Sidec Technologies AB, Sweden

Roundtable 4: How Do We Effectively Implement New Stagegate Criteria and Better Prioritize Projects within Our Portfolios?
Facilitator: James Resch, Ph.D., Director, Strategic Planning, Global Discovery Affairs, AstraZeneca

Roundtable 5: The Challenges, Risks and Rewards of Developing Multi-Indication Treatment Platforms
Facilitator: Jan Malek, PA Consulting

Roundtable 6: What Are the Risks and Rewards of Resurrecting Failed Compounds?
Facilitator: Paul Thonnard, Market Analyst, Lilly Forecasting, Eli Lilly & Co.

4:00 pm Networking Refreshment Break

PLENARY SESSION - ROUNDTABLE FINDINGS

4:30 pm Executive Panel: Roundtable Synopsis and Findings 
Each roundtable group will designate a leader to sit on a panel and present a short summary of their discussion. A moderator will then open a discussion amongst all attendees addressing the most critical questions facing the industry. 

5:45 pm Networking Cocktail Reception hosted by PA Consulting

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